中华生物医学工程杂志
中華生物醫學工程雜誌
중화생물의학공정잡지
CHINESE JOURNAL OF BIOMEDICAL ENGINEERING
2014年
6期
437-440
,共4页
张全斌%窦娟%李娇%马云霞%李鹏丽%郝子琪%周永安
張全斌%竇娟%李嬌%馬雲霞%李鵬麗%郝子琪%週永安
장전빈%두연%리교%마운하%리붕려%학자기%주영안
粉防己碱%氟康唑%念珠菌,热带
粉防己堿%氟康唑%唸珠菌,熱帶
분방기감%불강서%념주균,열대
Tetrandrine%Fluconazole%Candida tropicalis
目的 探讨粉防己碱抑制耐氟康唑热带念珠菌外排泵的机制.方法 通过MTT法确定24 h粉防己碱对耐氟康唑热带念珠菌的无细胞毒性剂量,并以此剂量处理5株耐氟康唑热带念珠菌.粉防己碱组(20 mg/L)及对照组(PBS)加入不同浓度的氟康唑(10~50 mg/L)处理48 h以测定MIC值.半定量PCR分析粉防己碱(20 mg/L)作用24 h前后,耐氟康唑热带念珠菌外排泵基因CDR1和MDR1转录水平的变化;流式细胞术检测粉防己碱(20 mg/L)作用24 h后对耐氟康唑热带念珠菌罗丹明123的蓄积能力的影响.结果 粉防己碱对耐氟康唑热带念珠菌的最大无细胞毒性剂量为20 mg/L.以此浓度处理5株耐氟康唑热带念珠菌,与对照组相比,MIC的范围由64(64~128)mg/L减少到32(24~64)mg/L(P<0.05).粉防己碱可以将耐氟康唑热带念珠菌CDR1和MDR1基因mRNA水平的表达由0.905±0.026及0.649±0.028分别下调至0.715±0.131和0.342±0.068(均P<0.05).粉防己碱作用后的耐氟康唑热带念珠菌对罗丹明123的蓄积量提升至(37.7±3.5)%,高于对照组的(16.3±2.2)%(P<0.05).结论 粉防己碱可以减少耐氟康唑热带念珠菌外排蛋白的表达,增加细胞内药物的蓄积,从而抑制氟康唑的耐药作用.
目的 探討粉防己堿抑製耐氟康唑熱帶唸珠菌外排泵的機製.方法 通過MTT法確定24 h粉防己堿對耐氟康唑熱帶唸珠菌的無細胞毒性劑量,併以此劑量處理5株耐氟康唑熱帶唸珠菌.粉防己堿組(20 mg/L)及對照組(PBS)加入不同濃度的氟康唑(10~50 mg/L)處理48 h以測定MIC值.半定量PCR分析粉防己堿(20 mg/L)作用24 h前後,耐氟康唑熱帶唸珠菌外排泵基因CDR1和MDR1轉錄水平的變化;流式細胞術檢測粉防己堿(20 mg/L)作用24 h後對耐氟康唑熱帶唸珠菌囉丹明123的蓄積能力的影響.結果 粉防己堿對耐氟康唑熱帶唸珠菌的最大無細胞毒性劑量為20 mg/L.以此濃度處理5株耐氟康唑熱帶唸珠菌,與對照組相比,MIC的範圍由64(64~128)mg/L減少到32(24~64)mg/L(P<0.05).粉防己堿可以將耐氟康唑熱帶唸珠菌CDR1和MDR1基因mRNA水平的錶達由0.905±0.026及0.649±0.028分彆下調至0.715±0.131和0.342±0.068(均P<0.05).粉防己堿作用後的耐氟康唑熱帶唸珠菌對囉丹明123的蓄積量提升至(37.7±3.5)%,高于對照組的(16.3±2.2)%(P<0.05).結論 粉防己堿可以減少耐氟康唑熱帶唸珠菌外排蛋白的錶達,增加細胞內藥物的蓄積,從而抑製氟康唑的耐藥作用.
목적 탐토분방기감억제내불강서열대념주균외배빙적궤제.방법 통과MTT법학정24 h분방기감대내불강서열대념주균적무세포독성제량,병이차제량처리5주내불강서열대념주균.분방기감조(20 mg/L)급대조조(PBS)가입불동농도적불강서(10~50 mg/L)처리48 h이측정MIC치.반정량PCR분석분방기감(20 mg/L)작용24 h전후,내불강서열대념주균외배빙기인CDR1화MDR1전록수평적변화;류식세포술검측분방기감(20 mg/L)작용24 h후대내불강서열대념주균라단명123적축적능력적영향.결과 분방기감대내불강서열대념주균적최대무세포독성제량위20 mg/L.이차농도처리5주내불강서열대념주균,여대조조상비,MIC적범위유64(64~128)mg/L감소도32(24~64)mg/L(P<0.05).분방기감가이장내불강서열대념주균CDR1화MDR1기인mRNA수평적표체유0.905±0.026급0.649±0.028분별하조지0.715±0.131화0.342±0.068(균P<0.05).분방기감작용후적내불강서열대념주균대라단명123적축적량제승지(37.7±3.5)%,고우대조조적(16.3±2.2)%(P<0.05).결론 분방기감가이감소내불강서열대념주균외배단백적표체,증가세포내약물적축적,종이억제불강서적내약작용.
Objective To explore the mechanism underlying inhibitory effect of tetrandrine on the efflux pump in fluconazole-resistant Candida tropicalis.Methods The non-cytotoxic dose of tetrandrine to Cadida tropicalis at 24 h was determined by MTT method.Tetrandrine by the determined dose was applied to five strains of fluconazole-resistant Candida tropicalis.The tetrandrine-treated group(20 mg/L)and the control group(PBS)of Candida tropicalis were then added with various concentrations of fluconazole(10-50 mg/L) for 48 h to determine the minimal inhibitory concentration (MIC).Semi-quantitative reverse transcription-PCR was used to examine the relative transcriptional level shift of CDR1 and MDR1 genes in these fluconazole-resistant strains before and after treatment with 20 mg/L tetrandrine for 24 h.Flow-cytometry was used to determine the effect of tetrandrine on rhodamine 123 accumulation capacity in Candida tropicalis at 24 h.Results The maximum non-cytotoxic dose of tetrandrine to Candida tropicalis was 20 mg/L as determined by MTT assay.Compared with the control group,in the 5 strains of fluconazole-resistant Candida tropicalis treated with maximum non-cytotoxic dose,the MIC of fluconazole decreased from 64(range 64-128)mg/L to 32(range 24-64)mg/L(P<0.05).Reverse transcription-PCR showed that the mRNA expression levels of CDR1 and MDR1 genes was reduced from 0.905±0.026 and 0.649±0.028 to 0.715±0.131 and 0.342±0.068,respectively(all P<0.05).After treatment with tetrandrine,the rhodamine 123 accumulation of fluconazole-resistant Candida tropicalis was elevated to(37.7 ± 3.5)%,compared with (16.3 ± 2.2)% in the controls (P<0.05).Conclusion Tetrandrine may down-regulate the expression of efflux pump genes and increase intracellular drug accumulation in fluconazole-resistant Candida tropicalis,thereby inhibiting the fluconazole resistance in this fungus.